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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649313Generated: October 25, 2026

Ammonium Hydroxide → 5-(3-Methylpentan-3-yl)-1,3,4-thiadiazol-2-amine

https://huagongshe.com/reaction/1649313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-Ethyl-2-methylbutyric acidHCID 29846—
ReactantThiosemicarbazideHCID 2723789—
Solvent1,4-DioxaneHCID 31275—
Product5-(3-Methylpentan-3-yl)-1,3,4-thiadiazol-2-amineHCID 1323426391.9%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution containing 13.0 g of 2-ethyl-2-methylbutyric acid and 9.1 g of thiosemicarbazide in 125 ml of dioxane was stirred and heated to 90° C. To the stirred reaction mixture was added dropwise over thirty minutes 15.3 g of phosphorous oxychloride. Following complete addition, the reaction mixture was heated at 90° C. for six hours. The mixture was then cooled to about 30° C. and added to 100 g of ice. The aqueous mixture was made alkaline by the addition of ammonium hydroxide, and the alkaline solution was extracted several times with ethyl acetate. The extracts were combined, washed with water, dried, and the solvent was removed by evaporation under reduced pressure to afford 17.0 g of 2-amino-5-(1-ethyl-1-methylpropyl)-1,3,4-thiadiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04416683
Source datasetuspto-grants-1983_11
ORD IDord-a84f06af9dff452c90b10adf40dd1c5d
Source noteuspto-grants-1983_11